Posttranscriptional orchestration of an anti-apoptotic program by HuR

Kotb Abdelmohsen, Ashish Lal, Ho Kim Hyeon, Myriam Gorospe

Research output: Contribution to journalReview articlepeer-review

212 Scopus citations

Abstract

The RNA-binding protein HuR can stabilize and/or regulate the translation of target mRNAs, thereby affecting the cellular responses to immune, proliferative, and damaging agents. Here, we discuss emerging evidence that HuR elicits a broad anti-apoptotic function through its influence on the expression of multiple target mRNAs. HuR was previously shown to bind to the mRNA encoding the apoptosome inhibitor prothymosin α (ProTaα) and enhanced its translation and cytoplasmic abundance. More recently, HuR was shown to increase the stability of a target mRNA encoding the pro-survival deacetylase SIRT1. The discovery that HuR likewise binds to and promotes the expression of mRNAs encoding Bcl-2 and Mcl-1, two major anti-apoptotic effectors, strongly supports HuR's role as a key upstream coordinator of a constitutive pro-survival program.

Original languageEnglish
Pages (from-to)1288-1292
Number of pages5
JournalCell Cycle
Volume6
Issue number11
DOIs
StatePublished - 1 Jun 2007
Externally publishedYes

Keywords

  • Bcl-2
  • ELAV
  • Mcl-1
  • mRNA turnover
  • mRNA-binding protein
  • ProTα
  • SIRT1
  • Translational control

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